A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613969



Internal ID21562274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85818864..85818864hg38UCSC Ensembl
chr3:85868014..85868014hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138924
SamplesHG02818
Known GenesCADM2, CADM2-AS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613969
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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